Differences in Efficacy and Safety Between Capecitabine and Infusional 5-Fluorouracil When Combined With Irinotecan for the Treatment of Metastatic Colorectal Cancer
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作者:
Montagnani, Francesco
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S Giuseppe Hosp, AUSL, Dept Med, Oncol Unit, I-50053 Florence, ItalyS Giuseppe Hosp, AUSL, Dept Med, Oncol Unit, I-50053 Florence, Italy
Montagnani, Francesco
[1
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Chiriatti, Antonella
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Univ Siena, Sch Med, Nurse Med Sch, I-53100 Siena, ItalyS Giuseppe Hosp, AUSL, Dept Med, Oncol Unit, I-50053 Florence, Italy
Chiriatti, Antonella
[2
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Licitra, Sara
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S Giuseppe Hosp, AUSL, Dept Med, Oncol Unit, I-50053 Florence, ItalyS Giuseppe Hosp, AUSL, Dept Med, Oncol Unit, I-50053 Florence, Italy
Licitra, Sara
[1
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Aliberti, Camillo
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Delta Hosp Lagosanto, Dept Radiol, Ferrara, ItalyS Giuseppe Hosp, AUSL, Dept Med, Oncol Unit, I-50053 Florence, Italy
Aliberti, Camillo
[3
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Fiorentini, Giammaria
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S Giuseppe Hosp, AUSL, Dept Med, Oncol Unit, I-50053 Florence, ItalyS Giuseppe Hosp, AUSL, Dept Med, Oncol Unit, I-50053 Florence, Italy
Fiorentini, Giammaria
[1
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机构:
[1] S Giuseppe Hosp, AUSL, Dept Med, Oncol Unit, I-50053 Florence, Italy
Background: Capecitabine is an oral fluoropyrimidine that is shown to have similar efficacy to 5-fluorouracil (5-FU) when used both alone and in combination with oxaliplatin in the treatment of colorectal cancer (CRC). Capecitabine and irinotecan combinations (XELIRI) have been developed for the treatment of this disease but randomized comparisons with standard infusional 5-FU and irinotecan (FOLFIRI) showed conflicting results. Patients and Methods: We searched the literature for randomized controlled trials comparing XELIRI to FOLFIRI for the treatment of metastatic colorectal cancer. Odds ratios with 95% confidence intervals were used to analyze dichotomous variables. Hazard ratios for progression and death were combined with an inverse variance method based on logarithmic conversion. The fixed-effect model and Mantel-Haenszel method were used. Heterogeneity was investigated with the Q-test and l(2.) Sensitivity analyses were performed. Results: Only 3 studies were identified, involving a total of 450 patients. XELIRI was associated with significantly shorter progression-free survival (PFS) and increased grade 3/4 gastrointestinal toxicities such as nausea, vomiting, and diarrhea. Severe neutropenia, however, was significantly more frequent with FOLFIRI. No differences in responses and febrile neutropenia events were observed. Conclusion: Our analysis suggest that the 2 regimens are not equivalent. XELIRI remains an option for the first-line treatment of metastatic CRC but FOLFIRI should be preferred as it confers more benefits in terms of PFS and induces fewer GI toxicities.
机构:
Univ Calif Los Angeles, Sch Med, Div Hematol Oncol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Sch Med, Div Hematol Oncol, Los Angeles, CA 90095 USA
Kabbinavar, Fairooz F.
Wallace, Joel F.
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Genentech Inc, San Francisco, CA 94080 USAUniv Calif Los Angeles, Sch Med, Div Hematol Oncol, Los Angeles, CA 90095 USA
Wallace, Joel F.
Holmgren, Eric
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Genentech Inc, San Francisco, CA 94080 USAUniv Calif Los Angeles, Sch Med, Div Hematol Oncol, Los Angeles, CA 90095 USA
Holmgren, Eric
Yi, Jing
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Genentech Inc, San Francisco, CA 94080 USAUniv Calif Los Angeles, Sch Med, Div Hematol Oncol, Los Angeles, CA 90095 USA
Yi, Jing
Cella, David
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机构:
Evanston NW Healthcare Res Inst, Ctr Outcomes Res & Educ, Evanston, IL USAUniv Calif Los Angeles, Sch Med, Div Hematol Oncol, Los Angeles, CA 90095 USA
Cella, David
Yost, Kathleen J.
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Evanston NW Healthcare Res Inst, Ctr Outcomes Res & Educ, Evanston, IL USAUniv Calif Los Angeles, Sch Med, Div Hematol Oncol, Los Angeles, CA 90095 USA
Yost, Kathleen J.
Hurwitz, Herbert I.
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Duke Univ, Durham, NC USAUniv Calif Los Angeles, Sch Med, Div Hematol Oncol, Los Angeles, CA 90095 USA